Product Details

SNP ID

rs555008

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:107899938 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTTTATCTCCTAAAATTCTATGC[A/C]CAGGCTCATGGTAGTAGCTTCTTCA

Phenotype

MIM: 610575

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

RSPO2 PubMed Links

Additional Information

For this assay, SNP(s) [rs77850474] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

RSPO2

Gene Name

R-spondin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282863.1	2513	UTR 3			NP_001269792.1
NM_001317942.1	2513	UTR 3			NP_001304871.1
NM_178565.4	2513	UTR 3			NP_848660.3
XM_011517018.1	2513	UTR 3			XP_011515320.1
XM_011517019.1	2513	UTR 3			XP_011515321.1
XM_017013395.1	2513	UTR 3			XP_016868884.1

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